Fig. 3
From: Genetic analysis assists diagnosis of clinical systemic disease in children with excessive hyperopia
The first figure shows the pedigree and IQCB1 mutations of case 1. I-1: the father, I-2: the mother, II-1: the case 1. M1: c.1090C > T, p.(R364*), M2: c.1333C > T, p.(R445*), N: Normal. The second figure shows the pedigree and PRSS56 mutations of case 2. I-1: the father, I-2: the mother (she did not previously undergo genetic testing), II-1: case 2. M1: c.632G > C, p.(C211S), M2: c.1066dup, p.(Q356Pfs), N: Normal